BIOTIME

Primary DI

06933260204038

Basic UDI-DI Code

B-06933260204038

Reference

BT0101201

Device Types

Single use

Regulation

Eu Ivdd

Classification

Eu Ivd General

Status

On The Market

Manufacturer

Xiamen Biotime Biotechnology Co., Ltd.

The Influenza A/B Antigen Rapid Test is a rapid lateral flow immunoassay for the qualitative detection and differentiation of Influenza A virus, including the present have-known subtypes, such as H1N1, H3N2, H5N1 and H7N9 and Influenza B virus, directly from nasal/throat/nasopharyngeal swab from individuals who have onset of symptoms, such as a sudden onset of fever, cough (usually dry), headache, muscle and joint pain and so on.

Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).